Late-onset hypogonadism

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Late-onset hypogonadism is a rare condition in older men, characterized by measurably low testosterone levels and clinical symptoms mostly of a sexual nature, including decreased desire for sex, fewer spontaneous erections, and erectile dysfunction.[1] It is the result of a gradual drop in testosterone; a steady decline in testosterone levels of about 1% per year is well documented in both men and women.[2][3]

Classification and terminology[edit]

Late-onset hypogonadism is an endocrine condition as well as a result of aging.[1]

The terms "male menopause" and "andropause" are used in the popular media and are misleading, as they imply a sudden change in hormone levels similar to what women experience in menopause.[4]

Symptoms, diagnosis, and screening[edit]

As of 2016, The International Society for the Study of the Aging Male defines late-onset hypogonadism as a series of symptoms in older adults related to testosterone deficiency that combines features of both primary and secondary hypogonadism; the European Male Aging Study (a prospective study of ~3000 men)[5] defined the condition by the presence of at least three sexual symptoms (e.g. reduced libido, reduced spontaneous erections, and erectile dysfunction) and total testosterone concentrations of less than 11 nmol/l (3.2 ng/ml) and free testosterone concentrations of less than 220 pmol/l (64 pg/ml).[1]

Some men present with the symptoms but with normal testosterone levels and some men with low testosterone levels have no symptoms; the reasons for this are not known.[1][6]

Some men in their late 40s and early 40's develop depression, loss of libido, erectile dysfunction, and other physical and emotional symptoms like irritability, loss of muscle mass and reduced ability to exercise, weight gain, lack of energy, difficulty sleeping, or poor concentration; many of these symptoms arise from a midlife crisis or as the results of a long term unhealthy life style (smoking, excess drinking, overeating, lack of exercise) and may be best addressed by lifestyle changes, therapy, or anti-depressants.[4]

If a person has symptoms of late-onset hypogonadism, testosterone is measured by taking blood in the morning on at least two days; while immunoassays are commonly used, mass spectrometry is more accurate and is becoming more widely available.[6] The meaning of the measurement is different depending on many factors that affect how testosterone is made and how it is carried in the blood. There will be Increased concentrations of proteins that bind testosterone in blood if the person is older, has hyperthyroidism, liver disease, or is taking anticonvulsant drugs (which are increasingly used for depression and various neuropathies), and there will be decreased concentrations of proteins that bind testosterone if the person is obese, has diabetes, has hypothyroidism, has liver disease, or is taking glucocorticoids or androgens, or progestins.[6] If levels are low, conditions that cause primary and secondary hypogonadism need to be ruled out.[6][7][8]

Due to difficulty and expense of testing, and the ambiguity of the results, screening is not recommended.[1][6] While some clinical instruments (standard surveys) had been developed as of 2016, their specificity was too low to be useful clinically.[1]


It is well documented that testosterone levels decline with aging at about 1% per year in both men and women after a certain age; the causes are not well understood.[1][2][3][9][10]


The significance of a decrease in testosterone levels is debated and its treatment with replacement is controversial. The Food and Drug Administration (FDA) stated in 2015 that neither the benefits nor the safety of testosterone have been established in older men with low testosterone levels.[11]

Testosterone replacement therapy should only be started if low levels have been confirmed;[7] in the US this is not done about 25% of the time, as of 2015.[8] Testosterone levels should also be monitored during therapy.[7]

Adverse effects[edit]

Adverse effects of testosterone supplementation may include increased cardiovascular events (including strokes and heart attacks) and deaths), especially in men over 65 and men with pre-existing heart conditions.[1] The risk that there CV risk of testosterone therapy is significant led the FDA to issue a requirement in 2015 that testosterone pharmaceutical labels include warning information about the possibility of an increased risk of heart attacks and stroke.[1][11] However, the data is mixed, and so The European Medicines Agency, the American Association of Clinical Endocrinologists, and the American College of Endocrinology have stated that there is no consistent evidence that testosterone therapy either increases or decreases cardiovascular risk.[1]

Other significant adverse effects of testosterone supplementation include acceleration of pre-existing prostate cancer growth; increased hematocrit, which can require venipuncture in order to treat; and, exacerbation of sleep apnea.[1]

Adverse effects may also include minor side-effects such as acne and oily skin, as well as, significant hair loss and/or thinning of the hair, which may be prevented with 5-alpha reductase inhibitors ordinarily used for the treatment of benign prostatic hyperplasia, such as finasteride or dutasteride.[12]

Exogenous testosterone may also cause suppression of spermatogenesis, leading to, in some cases, infertility.[1]


As of 2015, the evidence is inconclusive as to whether testosterone replacement therapy can help with erectile dysfunction in men with late-onset hypogonadism.[8] It appears that testosterone replacement therapy may benefit men with symptoms of frailty who have late-onset hypogonadism.[8]


The epidemiology is not clear. 20% of men in their 60s and 30% of men in their 70s have low testosterone;[2][8] around 5% of men between 70 years and 79 have both low testosterone and the symptoms, and so are diagnosed with late-onset hypogonadism.[2] The National Health Service describes it as rare.[4]


The impact of low levels of testosterone has been previously reported. In 1944, Heller and Myers identified symptoms of what they labeled the "male climacteric" including loss of libido and potency, nervousness, depression, impaired memory, the inability to concentrate, fatigue, insomnia, hot flushes, and sweating. Heller and Myers found that their subjects had lower than normal levels of testosterone, and that symptoms decreased dramatically when patients were given replacement doses of testosterone.[13][14]

Society and culture[edit]

Popular interest in the concept of "andropause" was fueled by the 1998 book Male Menopause, written by Jed Diamond, a lay person.[15] According to Diamond's view, andropause is a change of life in middle-aged men, which has hormonal, physical, psychological, interpersonal, social, sexual, and spiritual aspects. Diamond claims that this change occurs in all men, may occur as early as age 45 to 50 and more dramatically after the age of 70 in some men and that women's and men’s experience are somewhat similar phenomena.[16][17] The language of "andropause" and its supposed parallels with menopause have been rejected by the medical community.[4][18]

Thomas Perls and David J. Handelsman, in a 2015 editorial in the Journal of the American Geriatrics Society, say that between the ill-defined nature of the diagnosis and the pressure and advertising from drug companies selling testosterone and human growth hormone, as well as dietary supplement companies selling all kinds of "boosters" for aging men, the condition is overdiagnosed and overtreated.[19] Perls and Handelsman note that in the US, "sales of testosterone increased from $324 million in 2002 to $2 billion in 2012, and the number of testosterone doses prescribed climbed from 100 million in 2007 to half a billion in 2012, not including the additional contributions from compounding pharmacies, Internet, and direct-to-patient clinic sales."[19]

Research directions[edit]

As of 2016, research was necessary to find better ways to measure testosterone and to be better able understand the measurements in any given person, and to understand why some people with low testosterone do not present with symptoms and some with seemingly adequate levels do present with symptoms.[1] Research was also necessary to better understand the cardiovascular risks of testosterone replacement therapy in older men.[1]

A relationship between late-onset hypogonadism and risk of Alzheimers and some small clinical studies have been conducted to prevent Alzheimers in men with late-onset hypogonadism; os of 2009 results were inconclusive.[20]

See also[edit]


  1. ^ a b c d e f g h i j k l m n Dimopoulou, C; et al. (February 2016). "EMAS position statement: Testosterone replacement therapy in the aging male.". Maturitas. 84: 94–9. PMID 26614257. 
  2. ^ a b c d Samaras, N; Papadopoulou, MA; Samaras, D; Ongaro, F (2014). "Off-label use of hormones as an antiaging strategy: a review.". Clinical interventions in aging. 9: 1175–86. PMC 4116364free to read. PMID 25092967. 
  3. ^ a b Shifren, JL (October 2015). "Testosterone for midlife women: the hormone of desire?". Menopause (New York, N.Y.). 22 (10): 1147–9. PMID 26397145. 
  4. ^ a b c d "Male Menopause". NHS Choices. April 8, 2016. Retrieved October 7, 2016. 
  5. ^ Wu, FC; EMAS Study Group; et al. (8 July 2010). "Identification of late-onset hypogonadism in middle-aged and elderly men.". The New England Journal of Medicine. 363 (2): 123–35. PMID 20554979. 
  6. ^ a b c d e Basaria, S (5 April 2014). "Male hypogonadism.". Lancet (London, England). 383 (9924): 1250–63. PMID 24119423. 
  7. ^ a b c Bhasin, S; Cunningham, GR; Hayes, FJ; Matsumoto, AM; Snyder, PJ; Swerdloff, RS; Montori, VM; Task Force, Endocrine Society (June 2010). "Testosterone therapy in men with androgen deficiency syndromes: an Endocrine Society clinical practice guideline.". The Journal of clinical endocrinology and metabolism. 95 (6): 2536–59. PMID 20525905. 
  8. ^ a b c d e Seftel, AD; Kathrins, M; Niederberger, C (August 2015). "Critical Update of the 2010 Endocrine Society Clinical Practice Guidelines for Male Hypogonadism: A Systematic Analysis.". Mayo Clinic proceedings. 90 (8): 1104–15. PMID 26205546. 
  9. ^ "Could you have low testosterone?: MedlinePlus Medical Encyclopedia". NIH: Medline Plus. September 18, 2014. 
  10. ^ Huhtaniemi, I (2014). "Late-onset hypogonadism: current concepts and controversies of pathogenesis, diagnosis and treatment.". Asian journal of andrology. 16 (2): 192–202. PMC 3955328free to read. PMID 24407185. 
  11. ^ a b Staff (3 March 2015). "FDA Cautions About Using Testosterone Products for Low Testosterone Due to Aging; Requires Labeling Change to Inform of Possible Increased Risk of Heart Attack And Stroke". FDA. Retrieved 5 March 2015. . NEJM Perspective piece: Nguyen, CP; et al. (20 August 2015). "Testosterone and "Age-Related Hypogonadism"--FDA Concerns.". The New England journal of medicine. 373 (8): 689–91. PMID 26287846.  . Popular summary: Tavernise, Sabrina (March 3, 2015). "Drugs Using Testosterone Will Label Heart Risks". New York Times. Retrieved March 19, 2015. 
  12. ^ Grech, Anthony; Breck, John; Heidelbaugh, Joel (7 October 2016). "Adverse effects of testosterone replacement therapy: an update on the evidence and controversy". Ther Adv Drug Saf. 5 (5): 190–200. doi:10.1177/2042098614548680 – via PubMed Central. 
  13. ^ Gabrielsen, JS; Najari, BB; Alukal, JP; Eisenberg, ML (May 2016). "Trends in Testosterone Prescription and Public Health Concerns.". The Urologic clinics of North America. 43 (2): 261–71. PMID 27132584. 
  14. ^ Heller, CG; Myers, GB (21 October 1944). "The male climacteric, its symptomatology, diagnosis and treatment". Journal of the American Medical Association. 126 (8): 472. doi:10.1001/jama.1944.02850430006003. 
  15. ^ Diamond, Jed (1998). Male Menopause. Naperville, Ill: Sourcebooks. ISBN 1-57071-397-9. 
  16. ^ Diamond, Jed (2000). Surviving Male Menopause. A Guide for Women and Men. Naperville, Ill: Sourcebooks. ISBN 1-57071-433-9. 
  17. ^ Tan, Robert S. (2001). The andropause mystery: unraveling truths about the male menopause. Houston, Tex: AMRED Pub. ISBN 0-9707061-0-3. 
  18. ^ Gorski, David (November 25, 2013). ""Low T": The triumph of marketing over science « Science-Based Medicine". Science-Based Medicine. 
  19. ^ a b Perls, T; Handelsman, DJ (April 2015). "Disease mongering of age-associated declines in testosterone and growth hormone levels.". Journal of the American Geriatrics Society. 63 (4): 809–11. PMID 25809947. 
  20. ^ Cherrier, MM (2009). "Testosterone effects on cognition in health and disease.". Frontiers of hormone research. 37: 150–62. PMID 19011295. 

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